Investigation and Development of Novel Synthetic Approaches for Synthesis of Euxanthone and Derived Dyes

dc.contributor.author Cetin, M. Mustafa
dc.date.accessioned 2024-12-15T16:33:04Z
dc.date.available 2024-12-15T16:33:04Z
dc.date.issued 2024
dc.description.abstract The historical dye Indian yellow, derived from euxanthic acid formed from 1,7-dihydroxyxanthone (euxanthone) and methyl (tri-O-acetyl-alpha-d-glucopyranosyl bromide) uronate, has significantly influenced the art world due to its vibrant color and unique production process. Studying Indian yellow is important for its historical relevance and impact on various art forms, as well as the challenges in its synthetic production. Herein, this work investigates the synthesis of the two main components, a novel method for obtaining euxanthone, and attempts to produce euxanthic acid and Indian yellow. All key intermediates and desired compounds have successfully been synthesized with good to high isolated yields, and characterized using different analytical and spectroscopic techniques. A proposed mechanism for euxanthone synthesis via 2,6,2 ',5 '-tetramethoxybenzophenone formation is also offered. During this process, 2,7-dihydroxyxanthone has also been synthesized, revealing an equilibration reaction that produced three isomeric tetramethoxybenzophenones, confirmed by both GC/MS and NMR. Following the synthesis of euxanthone and clarification of the equilibration, the production of Indian yellow via euxanthic acid formation has further been explored. en_US
dc.description.sponsorship Research Foundation for the State University of New York; Department of Chemistry at the State University of New York (SUNY) College at Buffalo and Office of Undergraduate Research [MMC_SEED]; Kadir Has University; SUNY Research Foundation; SUNY College at Buffalo en_US
dc.description.sponsorship The author thanks to Prof M. Scott Goodman for his endless support in the discussion of the obtained results, sage advice, insightful criticism and discussion, and patient encouragement during this work. The author also thanks to the personnel in the Department of Chemistry at the State University of New York (SUNY) College at Buffalo and Office of Undergraduate Research for their assistance in the collection of the data and use of facilities. Financial support from the Kadir Has University (MMC_BAF and MMC_SEED) and the SUNY Research Foundation is gratefully acknowledged. This research was also supported by SUNY College at Buffalo and Kadir Has University computer laboratories and facilities. Special thanks go to the Fulbright-International Institute of Education for providing me this opportunity and supporting my education and career. Finally, the author greatly thanks to his wife Mine and sons Metehan Arda and Mert Kaan for willingly giving him time to complete this work. en_US
dc.identifier.doi 10.1039/d4ra06475e
dc.identifier.issn 2046-2069
dc.identifier.scopus 2-s2.0-85209356323
dc.identifier.uri https://doi.org/10.1039/d4ra06475e
dc.identifier.uri https://hdl.handle.net/20.500.12469/7091
dc.language.iso en en_US
dc.publisher Royal Soc Chemistry en_US
dc.relation.ispartof RSC Advances
dc.rights info:eu-repo/semantics/openAccess en_US
dc.subject [No Keyword Available] en_US
dc.title Investigation and Development of Novel Synthetic Approaches for Synthesis of Euxanthone and Derived Dyes en_US
dc.type Article en_US
dspace.entity.type Publication
gdc.author.institutional Cetin, M. Mustafa
gdc.author.scopusid 57210592507
gdc.author.wosid Cetin, M. Mustafa/ABD-4269-2020
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gdc.description.department Kadir Has University en_US
gdc.description.departmenttemp [Cetin, M. Mustafa] Kadir Has Univ, Fac Engn & Nat Sci, TR-34083 Cibali, Istanbul, Turkiye en_US
gdc.description.endpage 35609 en_US
gdc.description.issue 48 en_US
gdc.description.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
gdc.description.scopusquality Q1
gdc.description.startpage 35601 en_US
gdc.description.volume 14 en_US
gdc.description.woscitationindex Science Citation Index Expanded
gdc.description.wosquality Q2
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gdc.identifier.pmid 39512647
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gdc.oaire.keywords Chemistry
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